Methods and Biomarkers for the Detection of Dengue Hemorrhagic Fever

a biomarker and dengue hemorrhagic fever technology, applied in the field of methods and biomarkers for the detection of dengue hemorrhagic fever, can solve the problems of limiting the routine application of these tests, no dhf drug therapy or vaccine, and 5 billion people at risk of dengu

Active Publication Date: 2013-01-03
BOARD OF RGT THE UNIV OF TEXAS SYST
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Dengue remains an international public health problem affecting urban populations in tropical and sub-tropical regions, where it is currently estimated that about 2.5 billion people are at risk of dengue infection.
DHF is particularly associated with capillary leakage, hemorrhage, circulatory shock, and representing life-threatening complication.
Currently, there is no drug therapy or vaccine for DHF.
Several factors limit routine application of these tests, including the timing of specimen c...

Method used

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  • Methods and Biomarkers for the Detection of Dengue Hemorrhagic Fever
  • Methods and Biomarkers for the Detection of Dengue Hemorrhagic Fever
  • Methods and Biomarkers for the Detection of Dengue Hemorrhagic Fever

Examples

Experimental program
Comparison scheme
Effect test

example 1

Identification of Biomarkers of DHF and Nonparametric DHF Modeling

[0044]To identify differentially expressed proteins associated with DHF, a reproducible, novel pre-separation fractionation method is developed, and is termed the biofluid analysis platform (BAP). BAP takes advantage of high recovery and quantitative size exclusion fractionation, followed by quantitative saturation fluorescence labeling, two dimensional gel electrophoresis (2-DE), and LC-MS / MS (liquid chromatography-tandem mass spectrometry) protein identification to identify differentially expressed proteins associated with DHF.

[0045]Plasma samples from 53 volunteers (42 DF and 13 DHF) with initial clinical presentation of dengue infection were obtained and subjected to focused and discovery-based proteomic using ELISA and BAP.

[0046]Demographics, clinical laboratory measurements, 9 cytokines and 419 plasma proteins at the time of initial presentation were compared between the outcomes of dengue fever and dengue hemor...

example 2

DHF MARS Detection Model Validation

[0070]The performance of the MARS predictor of DHF was assessed using several approaches. First, the overall accuracy of the model on the data set was analyzed by minimizing classification error using cross-validation. The model accuracy produced 100% accuracy for both DHF and DF classification (Table IV(B)). Another evaluation of the model performance is seen by analysis of the area under the Receiver Operating Characteristic (ROC) curve (AUC), where Sensitivity vs. one-Specificity was plotted. In the ROC analysis, a diagonal line starting at zero indicated that the output was a random guess, whereas an ideal classifier with a high true positive rate and low false positive rate will curve positively and strongly towards the upper left quadrant of the plot (21). The AUC is equivalent to the probability that two cases, one chosen at random from each group, are correctly ordered by the classifier (22). In the DHF MARS model, an AUC of 1.000 is seen (...

example 3

Linear Model for DHF Prediction

[0077]Although the nonparametric modeling method of example 2 has achieved great accuracy in identifying dengue infected patients who are at risk for developing DHF, the clinical application of this biomarker panel will require development of accurate methods for quantification of modified plasma proteins that can be adapted and disseminated into clinical laboratories, especially in those endemic areas. Therefore, it is important to have an early DHF detection model that is based solely on the combinations of clinical and accessible laboratory tests.

Sample Collection and Preparation

[0078]An active surveillance for dengue diseases study was conducted in Maracay, Venezuela. Subjects are enrolled if presented with a new fever equal to or greater than 38° C. accompanied by two or more of the signs and symptoms consistent with dengue virus infection including: myalgia, arthralgia, leucopenia, rash, headache, lymphoadenopathy, nausea, vomiting, positive tour...

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PUM

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Abstract

The present invention provides methods for detecting, analyzing, and identifying biomolecules used to identifying patient with dengue-like symptom who are at risk of DHF. The inventive method comprises detecting in a sample from a subject dengue infected patient one or more biomarkers selected from the group consisting of IL-10, fibrinogen, C4A, immunoglobulin, tropomyosin, and three isoforms of albumin, and which are used in a predictive MARS model to detect patients with risk of developing DHF.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This application claims priority to U.S. provisional application No. 61 / 493,923 filed on Jun. 6, 2011.BACKGROUND OF THE INVENTION[0002]Dengue remains an international public health problem affecting urban populations in tropical and sub-tropical regions, where it is currently estimated that about 2.5 billion people are at risk of dengue infection. Dengue virus is a single positive-stranded RNA virus of the family Flaviviridae; genus Flavivirus, which is transmitted among humans primarily by Aedes aegypti mosquitoes. In humans, dengue infection can produce diseases of a wide spectrum of severity, from asymptomatic to flu-like dengue fever (DF), to life-threatening dengue hemorrhagic fever (DHF), or dengue shock syndrome (DSS). DHF is particularly associated with capillary leakage, hemorrhage, circulatory shock, and representing life-threatening complication.[0003]Due to a number of factors, including increasing urbanization and globalizatio...

Claims

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Application Information

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IPC IPC(8): C40B30/04G01N33/566C40B40/10A61P7/04A61K33/00A61P29/00A61P31/12C12Q1/70A61K35/14
CPCG01N33/564G01N33/56983G01N33/6869G01N2333/5428G01N2333/4716G01N2333/55G01N2333/185A61P7/04A61P29/00A61P31/12G01N33/6851G01N2333/47G01N2333/76G01N2800/26Y02A50/30
Inventor KOCHEL, TADEUSZNORES GARCIA, JOSEFINABRASIER, ALLANRECINOS, ADRIANWIKTOROWICZ, JOHN E.SPRATT, HEIDIJU, HYUNSU
Owner BOARD OF RGT THE UNIV OF TEXAS SYST
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